COMPREHENSIVE SHOULDER 110005298

GUDID 00880304568174

Biomet Orthopedics, LLC

Implant handling forceps, scissors-like

• Primary Device ID: 00880304568174
• NIH Device Record Key: ba073c20-fb2e-4214-9ff0-4bb680b5b554
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COMPREHENSIVE SHOULDER
• Version Model Number: 110005298
• Catalog Number: 110005298
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304568174 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130390

FDA Product Code

• KWT: PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00880304568174]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-05-15
• Device Publish Date: 2016-10-28

On-Brand Devices [COMPREHENSIVE SHOULDER]

• 00880304568181: 110005302
• 00880304568174: 110005298
• 00880304568167: 110005294
• 00880304568150: 110005291
• 00880304568143: 110005287
• 00880304568136: 110005285
• 00880304568129: 110005283
• 00880304568112: 110005281
• 00880304568105: 110005273
• 00880304567955: 110005240
• 00880304567948: 110005237
• 00880304469563: 595505